JPH02138400A - Production of reclaimed leather - Google Patents
Production of reclaimed leatherInfo
- Publication number
- JPH02138400A JPH02138400A JP29191688A JP29191688A JPH02138400A JP H02138400 A JPH02138400 A JP H02138400A JP 29191688 A JP29191688 A JP 29191688A JP 29191688 A JP29191688 A JP 29191688A JP H02138400 A JPH02138400 A JP H02138400A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- leather
- parts
- emulsion
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000010985 leather Substances 0.000 title claims abstract description 41
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 239000000839 emulsion Substances 0.000 claims abstract description 39
- 239000011347 resin Substances 0.000 claims abstract description 34
- 229920005989 resin Polymers 0.000 claims abstract description 34
- 239000002699 waste material Substances 0.000 claims abstract description 30
- 239000000178 monomer Substances 0.000 claims abstract description 24
- 125000000129 anionic group Chemical group 0.000 claims abstract description 21
- 239000002002 slurry Substances 0.000 claims abstract description 14
- 239000000203 mixture Substances 0.000 claims abstract description 10
- 125000001246 bromo group Chemical group Br* 0.000 claims abstract description 9
- 229920001577 copolymer Polymers 0.000 claims abstract description 8
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims abstract description 7
- 102000004169 proteins and genes Human genes 0.000 claims abstract description 7
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 7
- 125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 6
- 239000012874 anionic emulsifier Substances 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 11
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 5
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 3
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 claims description 3
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 claims description 2
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 14
- 238000005452 bending Methods 0.000 abstract description 3
- XJELOQYISYPGDX-UHFFFAOYSA-N ethenyl 2-chloroacetate Chemical compound ClCC(=O)OC=C XJELOQYISYPGDX-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000835 fiber Substances 0.000 description 17
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
- 239000010902 straw Substances 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 239000002649 leather substitute Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- -1 cationic chromium salts Chemical class 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- 230000002776 aggregation Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 239000012784 inorganic fiber Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- ORGWANBFJHCASW-UHFFFAOYSA-N C=CC(=O)OCCNC(=O)CCl Chemical compound C=CC(=O)OCCNC(=O)CCl ORGWANBFJHCASW-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 125000003158 alcohol group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000010009 beating Methods 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- HQTJNEILVZMZPN-UHFFFAOYSA-N n-[[(2-chloroacetyl)amino]methyl]prop-2-enamide Chemical compound ClCC(=O)NCNC(=O)C=C HQTJNEILVZMZPN-UHFFFAOYSA-N 0.000 description 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 2
- 239000012875 nonionic emulsifier Substances 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- DRROLYJXLSRMCR-UHFFFAOYSA-N 2-[(2-chloroacetyl)amino]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCNC(=O)CCl DRROLYJXLSRMCR-UHFFFAOYSA-N 0.000 description 1
- JUMQDBKTEFHFJW-UHFFFAOYSA-N 2-bromoethenyl acetate Chemical compound CC(=O)OC=CBr JUMQDBKTEFHFJW-UHFFFAOYSA-N 0.000 description 1
- XYPHEDNABNFRBL-UHFFFAOYSA-N 2-chloroethenyl acetate Chemical compound CC(=O)OC=CCl XYPHEDNABNFRBL-UHFFFAOYSA-N 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- NDYJLXDYJDOXES-UHFFFAOYSA-N C(=O)(NCCOC(=O)CCl)C=C Chemical compound C(=O)(NCCOC(=O)CCl)C=C NDYJLXDYJDOXES-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000283986 Lepus Species 0.000 description 1
- YZMNLRBZSYGPRL-UHFFFAOYSA-N OS(O)(=O)=O.CCCCCCCCCC1=CC=C(O)C=C1 Chemical compound OS(O)(=O)=O.CCCCCCCCCC1=CC=C(O)C=C1 YZMNLRBZSYGPRL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical group CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000013001 point bending Methods 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
Landscapes
- Treatment And Processing Of Natural Fur Or Leather (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、製本工程で発生するクロムなめしされた革の
シェービング屑を用いて再生皮革を製造する方法に関す
る。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for producing recycled leather using shaving waste from chrome-tanned leather generated during the bookbinding process.
クロムなめしされたシェービング屑を主成分とする開繊
維の水分散液に、アニオン性樹脂水性エマルジョン接着
剤を配合したスラリーを湿式抄造してシート状にし、こ
れを乾燥して再生皮革を製造することは公知である(特
公昭59−560号、同59−33,160号、特開昭
57−154.500号、同58−93.800号、同
57−149,566号)。A slurry containing an aqueous anionic resin emulsion adhesive mixed with an aqueous dispersion of open fibers whose main component is chrome-tanned shaving waste is wet-formed into a sheet, which is then dried to produce recycled leather. are publicly known (Japanese Patent Publication No. 59-560, 59-33,160, 57-154.500, 58-93.800, 57-149,566).
これら公知技術において、アニオン性樹脂エマルジョン
は接着剤の機能の他に、得られる再生皮革に耐水性、成
形性を付与する。In these known techniques, the anionic resin emulsion not only functions as an adhesive but also provides water resistance and moldability to the resulting recycled leather.
しかしながら一般に、りOJ−なめしされたシェービン
グ屑は、カチオン性のクロム塩でなめし処理されるもの
が多く、皮のカルボキシル基は封鎖され塩基性基が活性
化されていることにより、そこにアニオン性樹脂エマル
ジョンの接着剤を加えた場合に、このアニオン性接着剤
とシェービング屑との結合が非常に早くな抄接着剤が皮
繊維の表面で急激に結合して接着剤を媒体とした皮繊維
同志の塊状物が形成され、湿式法による抄紙が事実上困
難になる。However, in general, OJ-tanned shaving waste is often tanned with cationic chromium salts, and the carboxyl groups of the skin are blocked and the basic groups are activated, so there is anionic shavings. When a resin emulsion adhesive is added, the anionic adhesive and the shaving waste bond rapidly on the surface of the leather fibers, causing the leather fibers to bond together using the adhesive as a medium. Agglomerates are formed, making papermaking by the wet process virtually difficult.
それ故、クロムなめしされ九シェービング清水分散液と
アニオン性樹脂水性エマルジョンを混合した場合の凝集
を防ぐ方法として前述の特許公報群は、s奈宝9−33
,160号では、50〜95%のクロムなめし藁屑に、
5〜50%の微細石綿又はカチオン性微細無機繊維とを
水中で混合したものにアニオン性樹脂エマルジョンを添
加すると湿式抄紙出来るとしている。これは、カチオン
系無機繊維表面にアニオン性樹脂エマルジョンヲ藁屑よ
抄先に凝集させ、見掛上革との凝集の確率を下げている
。Therefore, as a method for preventing agglomeration when mixing a chromium-tanned 9-shaving clean water dispersion and an anionic resin aqueous emulsion, the aforementioned patent publication group s Naho 9-33
, No. 160, 50-95% chrome tanning straw waste,
It is said that wet papermaking is possible by adding an anionic resin emulsion to a mixture of 5 to 50% fine asbestos or cationic fine inorganic fibers in water. This causes the anionic resin emulsion to aggregate on the surface of the cationic inorganic fibers at the tip of the paper, reducing the apparent probability of aggregation with the leather.
との方法では、革以外の成分を加える必要がちる為品質
の変化がある。With this method, there is a change in quality because it is necessary to add ingredients other than leather.
%$t−149,56s号では皮革屑にラテックス、(
アクリルを除くエマルジョン)を加えてシート状に抄造
するとあるがアニオン活性のアクリル系樹脂エマルジョ
ンではクロムなめし革では凝集を起こしてしまう。しか
しながらアクリル系樹脂は、硬さ、柔軟性、耐候性、耐
久性においてラテックス系にくらべすばらしいものがあ
る。%$t-149,56s issue has leather scraps and latex (
The paper is made into a sheet by adding an emulsion (excluding acrylic), but the anion-activated acrylic resin emulsion causes agglomeration in chrome tanned leather. However, acrylic resins have superior hardness, flexibility, weather resistance, and durability compared to latex resins.
β1
萄#s 7−154.500号、同58−93,800
号はシェービング屑を製紙用繊維と混抄するに際し、ア
ニオン性アクリル酸エステル樹脂エマルジ剤を加えて、
あらかじめ凝集物スラリーとし、これを藁屑スラリーと
混合することによ抄、バインダーと革繊維との不均一性
を少しでも解消することを試みているが作業の煩雑さと
、やはり均一性に問題がある。β1 萄#s 7-154.500, 58-93,800
In this issue, when mixing shaving waste with papermaking fibers, an anionic acrylic ester resin emulsion agent is added,
Attempts have been made to eliminate the non-uniformity between the binder and the leather fibers by making an aggregate slurry in advance and mixing it with the straw waste slurry, but the process is complicated and there are still problems with uniformity. be.
かかる従来の欠点を改良する方法として、先に我々は、
クロムなめしされたシェービング屑解繊物と、α、β−
不飽和カルボン酸に基づくカルボキシル基(−COOH
)を1.4 X 10 モル以下の割合で含有するア
ニオン性樹脂水性エマルジョンを含有するスラリーから
再生皮革を製造する方法を提案した(峙願昭62−10
0827号)。As a method to improve such conventional drawbacks, we first
Chrome-tanned shaving waste defibrated material, α, β-
Carboxyl group based on unsaturated carboxylic acid (-COOH
proposed a method for producing recycled leather from a slurry containing an aqueous anionic resin emulsion containing 1.4 x 10 moles or less of
No. 0827).
この方法によると抄紙して再生皮革を生成するスラリー
の貯蔵安定性が良好であり、また強靭な再生皮革が得ら
れる利点がある。This method has the advantage that the slurry from which recycled leather is produced by papermaking has good storage stability and that tough recycled leather can be obtained.
この先願の方法によると、エマルジョン樹脂のカルボキ
シル基(−COOH’)が反応するのは、なめし藁屑の
たん白質のアミノ基(−NI(2’)と反応する程度で
あるから、人工皮革に強度をもたらすために屑の繊維長
の長い(3〜7 m )ものを使用する必要があり九。According to the method of this previous application, the carboxyl group (-COOH') of the emulsion resin reacts to the extent that it reacts with the amino group (-NI(2')) of the protein in the tanning straw, so it is not suitable for artificial leather. It is necessary to use long fiber length (3-7 m) of waste to provide strength.
(たん白質) (結合剤)
しかし、繊維長の長いものを使用する場合、藁屑の分散
が困難で、均一なスラリーを得ることができない問題が
ある。(Protein) (Binder) However, when long fibers are used, it is difficult to disperse the straw waste, making it impossible to obtain a uniform slurry.
繊維長の短かい(3■以下)屑を用いると抄紙した人工
皮革の折9曲げ強度が低い。If waste with short fiber length (3 cm or less) is used, the folding strength of the paper-made artificial leather will be low.
本発明は、繊維長の長い屑繊維を用いても短い屑繊維を
用いても折り曲げ強度が良好な人工皮革を与えることを
目的とする。An object of the present invention is to provide artificial leather that has good bending strength regardless of whether long or short waste fibers are used.
本発明においては、バインダーのアニオン性共重合体水
性エマルジョンとして、なめし革屑のたん白質の−NH
z、−8H,−COOH,−CON市等の極性基と反応
する・・−ゲン基(−α、−13r )を有する共重合
本水性エマルジョンを用いること(より短繊維長のなめ
し革屑を用いてもバインダーのハロゲン基のたん白質の
極性基と結合が多く形成されるので折り曲げ強度の高い
人工皮革が得られる。In the present invention, as an aqueous emulsion of an anionic copolymer as a binder, -NH
Using a copolymerized aqueous emulsion with -gen groups (-α, -13r) that reacts with polar groups such as z, -8H, -COOH, -CON (using tanned leather scraps with shorter fiber length) However, since many bonds are formed between the halogen group of the binder and the polar group of the protein, artificial leather with high bending strength can be obtained.
即ち、本発明は、クロムなめしされた革のシェービング
を主成分とする滑層繊物と、革のたん白質と反応するク
ロル基又はブロム基(−〇、−Br)を有する不飽和単
量体O,S〜10重量シと他の不飽和単量体99.5〜
90!f1%とを共重合させて得た共重合体のアニオン
性樹脂水性エマルジョンを含有するスラリーを抄紙して
再生皮革を製造する方法を提供するものである。That is, the present invention is directed to a smooth fiber whose main component is chrome-tanned leather shavings, and an unsaturated monomer having a chloro group or a bromine group (-〇, -Br) that reacts with the protein of the leather. O, S~10 by weight and other unsaturated monomers 99.5~
90! The present invention provides a method for producing recycled leather by paper-making a slurry containing an aqueous anionic resin emulsion of a copolymer obtained by copolymerizing with f1%.
(シェービング屑)
クロムなめしされたシェービング屑は粒度均整化された
もので、乾燥状態でビータ−又はレファイナーの如き叩
解機で解繊処理、または水中で叩解機で解繊処理された
ものである。シェービング屑の一部をタンニンなめし革
屑やバルブファイバーや無機繊維、樹脂線維におきかえ
てもよい。(Shaving waste) Chrome-tanned shaving waste has a uniform particle size, and is defibrated in a dry state using a beater such as a beater or refiner, or defibrated in water using a beater. A portion of the shaving waste may be replaced with tanned leather waste, valve fiber, inorganic fiber, or resin fiber.
この十分に解繊処理されたシェービング屑は水中におい
て粥状のぬるぬるしたものである。このシェービング屑
と水の混合物に、アニオン性樹脂水性エマルジョンを加
える。This fully defibrated shaving waste becomes slimy like gruel in water. An anionic resin aqueous emulsion is added to this shaving waste and water mixture.
(アニオン性樹脂水性エマルジョン)
再生皮革に形状保持性、耐水性、柔軟性又は剛性を付与
するアニオン性樹脂水性エマルジョンは、クロル基また
はブロム基含有不飽和単量体O,S〜10重量%を含有
する不飽和単量体を、ドデシルベンゼンスルホン酸ンー
ダ、p−ノニルフェノールの硫酸半エステル等のアニオ
ン性界iff 活性剤0.1〜5重量%、ノニオン性界
面活性剤0〜5重ft%および過硫酸カルシウムの存在
下に乳化重合して得られる共重合体の樹脂エマルジョン
である。(Aqueous anionic resin emulsion) The aqueous anionic resin emulsion that imparts shape retention, water resistance, flexibility, or rigidity to recycled leather contains ~10% by weight of unsaturated monomers containing chlorine or bromine groups. Containing unsaturated monomers, anionic surfactants such as dodecylbenzenesulfonic acid and p-nonylphenol sulfuric acid half ester, 0.1 to 5% by weight of nonionic surfactants, and 0 to 5% by weight of nonionic surfactants. This is a resin emulsion of a copolymer obtained by emulsion polymerization in the presence of calcium persulfate.
なめし革屑のたん白質と反応するハロゲン基を有する不
飽和単量体としては、
式、
〔式中、RはRまたはC1(31R1はクロル基あるい
はブロモ基を1つ以上含むアルコール残基である〕
で示される2、3−ジクCIOプロピルアクリレート、
2.3−ジクロログロビルメタクリレート等;式、
O
〔式中、Xは(::1. Brより選ばれた〕・ロゲ
ン基を、YはH,CH3、CNより選ばれた基である〕
で示されるモノクロル酢酸ビニル、モノブロム酢酸ビニ
ル、α−シアノモノクロル酢酸ビニル、α−シアノモノ
ブロム酢酸ビニル等:
式、
RO0
〔式中、RはHまたはCH3: Xは(1)式の定義と
同じ〕
で示される(N−モノフロロアセトアミドメチル)アク
リルアミド、(N−モノクロロアセトアミドメチル)ア
クリルアミド、(N−モノブロムアセトアミトメデル)
アクリルアミド、およびこれらのメタクリルアミド相当
物;
式、
に υ
で示される(N−モノクロルアセトキシエチル)アクリ
ルアミド、(N−モツプロムアセトキシエチル)アクリ
ルアミド、(N−モノクロルアセトキシエチル)メタク
リルアばド等;
式、
ROO
で示される2−モノクロルアセトアミドエチルアクリル
酸エステル、2−モノクロルアセトアミドエチルメタク
リル酸エステル、2−モノクロルアセトアミドエチルア
クリル酸エステル等が用いられる。The unsaturated monomer having a halogen group that reacts with the protein of tanned leather scraps has the following formula: [In the formula, R is R or C1 (31R1 is an alcohol residue containing one or more chloro group or bromo group)] 2,3-dicCIOpropyl acrylate represented by
2.3-dichloroglobil methacrylate, etc.; formula, O [wherein,
Monochlorovinyl acetate, monobromovinyl acetate, α-cyanomonochlorovinyl acetate, α-cyanomonobromovinyl acetate, etc.: Formula, RO0 [wherein, R is H or CH3: X is the same as the definition of formula (1) ] (N-monochloroacetamidomethyl)acrylamide, (N-monochloroacetamidomethyl)acrylamide, (N-monobromoacetamidomethyl)
Acrylamide and their methacrylamide equivalents; (N-monochloroacetoxyethyl)acrylamide, (N-motupromacetoxyethyl)acrylamide, (N-monochloroacetoxyethyl)methacrylabad, etc., represented by υ in the formula; , 2-monochloroacetamidoethyl acrylate, 2-monochloroacetamidoethyl methacrylate, 2-monochloroacetamidoethyl acrylate and the like represented by ROO are used.
この・・ロゲン基を有する不飽和単量体は0.5〜10
重険%、好ましくは1.5〜5゜O重@%の割合で用い
る。0.5重t%未満ではエマルジョン共重合体樹脂の
バインダー効果が不十分でらる。10重量%を越えては
乳化重合が困難であるし、高価なこの・・ロゲン基(−
C1,−Br)含有不飽和単量体を用いることは人工皮
革の生産コストが高くなり不利である。This unsaturated monomer having a rogene group is 0.5 to 10
It is used in a ratio of 1.5 to 5°O weight%, preferably 1.5 to 5°O weight%. If it is less than 0.5% by weight, the binder effect of the emulsion copolymer resin will be insufficient. If it exceeds 10% by weight, emulsion polymerization is difficult, and this expensive...
The use of C1,-Br)-containing unsaturated monomers is disadvantageous because it increases the production cost of artificial leather.
他の不飽和単量体としては、メタクリル酸n・プロピル
(Tg81C)、スチレン(100℃)、アクリロニト
リル(100℃)、メタクリル酸メチル(105℃)、
メタクリル酸(130℃)、イタコン酸(130℃)、
アクリルアミド(153℃)、アクリル酸2−エチルヘ
キシル(Tg−85℃)、アクリA−酸1111プデル
(−54’C)、アクリル酸エチル(−22℃)、アク
リル酸インプロピル(−50)、メタクリル酸2−工t
ルヘキシ・ル(−5℃)、アクリル酸n・プロピル(8
℃)、メタクリル酸n拳ブデル(20℃)、酢酸ビニル
(30℃)、アクリル酸t−ブチル(45℃)、メタク
リル酸2−ヒドロキシニブル(55℃)、メタクリル酸
メチル(85C)、メタクリル酸インブデル(67℃)
、塩化ビニル(79℃)、塩化ビニリデン(−180)
、エチレン等が単独で、または二種以上混合して用いら
れる(括弧内の数字は、これらビニル単量体のホモ重合
体のガラス転移点である)。また、式
%式%
〔式中、RはHまたはcu、:R1はリン酸基を含むア
ルコール残基である〕
で示される2−アシッドホスホキシエチルメタクリレー
ト、2−アシッドホスホキシプロピルメタクリレート等
も0〜5重t%用いられる。Other unsaturated monomers include n-propyl methacrylate (Tg81C), styrene (100°C), acrylonitrile (100°C), methyl methacrylate (105°C),
Methacrylic acid (130℃), itaconic acid (130℃),
Acrylamide (153°C), 2-ethylhexyl acrylate (Tg -85°C), acrylic A-acid 1111 pudel (-54'C), ethyl acrylate (-22°C), impropyl acrylate (-50), methacryl acid 2-t
n-propyl acrylate (-5°C), n-propyl acrylate (8
), Budel methacrylate (20°C), vinyl acetate (30°C), t-butyl acrylate (45°C), 2-hydroxynibble methacrylate (55°C), methyl methacrylate (85C), methacrylic acid Inbudel (67℃)
, vinyl chloride (79℃), vinylidene chloride (-180)
, ethylene, etc. are used alone or in combination of two or more types (the numbers in parentheses are the glass transition points of homopolymers of these vinyl monomers). In addition, 2-acid phosphoxyethyl methacrylate, 2-acid phosphoxypropyl methacrylate, etc. represented by the formula % formula % [wherein R is H or cu, and R1 is an alcohol residue containing a phosphoric acid group] 0 to 5% by weight is used.
これら単i本の種類、使用縫は、得られるエマルジョン
の使用温度を考慮して、得られる樹脂のガラス転移点を
目安として決定する。The type of these single pieces and the stitches to be used are determined by considering the usage temperature of the resulting emulsion and using the glass transition point of the resulting resin as a guide.
本発明においては、皮膜化の面から造膜温度が30℃以
下、皮膜の硬さ、ベタツキによる汚れ等を考慮して造膜
1度が一10℃以上のエマルジョンが好ましい。又、二
種以上のエマルジョンをブレンドして便用しても良い。In the present invention, from the viewpoint of forming a film, it is preferable to use an emulsion in which the film forming temperature is 30° C. or lower, and the film forming temperature is 110° C. or higher in consideration of the hardness of the film, stains due to stickiness, etc. Alternatively, two or more types of emulsions may be blended for use.
また、再生皮革を賦型する場合は、ガラス転移点が30
〜80℃の樹脂の水性エマルジョンが好ましい。エマル
ジョンの樹脂のTgが高くなると造膜の為の加熱による
革繊維の劣化と招くので、この点を考慮して樹脂のTg
の選定が必要になる。In addition, when molding recycled leather, the glass transition point is 30
An aqueous emulsion of the resin at ~80°C is preferred. If the Tg of the resin in the emulsion becomes high, the leather fibers will deteriorate due to heating for film formation.
It is necessary to select
又この場合藁屑の繊維長は長いのが好ましい。又、エマ
ルジョン樹脂!I変は20〜55重量%の本のが通常使
用される。又、消泡剤、分散剤、増貼剤、凍結防止剤、
造膜助剤、可塑剤、着色剤、充填剤、香料等をエマルジ
ョンに加えても良い。In this case, it is preferable that the straw waste has a long fiber length. Also, emulsion resin! Variant I is usually used in amounts of 20 to 55% by weight. In addition, antifoaming agents, dispersants, thickeners, antifreeze agents,
Coating aids, plasticizers, colorants, fillers, fragrances, etc. may be added to the emulsion.
好、ましい共重合体水性エマルジョンは、(8)クロル
基またはブロム基含有不飽和単量体0.5〜lO重陸シ
〜)アクリル酸アルキルエステル(アルキル基の炭素数
は2〜8)
40〜55重険シ
(C)メタクリル酸メチル、スチレンおよびアクリロニ
トリルより選ばれた単量体
30〜55重l1%
1)N−フェニル!レイミド、N−メチロールアクリル
アミド、アクリルアミド、メタクリルアミド、2−ヒド
ロキシアルキルアクリレート(アルキル基の炭素数は2
〜4)より選ばれた不飽和単殿体
θ〜lO重量%
(e)α、β−不飽和カルボン酸
0〜0.3重量%
よりなる不飽和単量体混合物100重量部を、アニオン
性乳化剤0.1〜5重量部およびノニオン性乳化剤0〜
5重量部の存在下に例えば過硫酸カルシウムの様な重合
触媒を用いて乳化重合して得られる造膜鑞度が一10〜
+80℃のものである。A preferable aqueous copolymer emulsion includes (8) an unsaturated monomer containing a chloro group or a bromine group (0.5 to 1 O), an acrylic acid alkyl ester (the number of carbon atoms in the alkyl group is 2 to 8); 40-55 weight (C) Monomer selected from methyl methacrylate, styrene and acrylonitrile 30-55 weight l1% 1) N-phenyl! Reimide, N-methylolacrylamide, acrylamide, methacrylamide, 2-hydroxyalkyl acrylate (the number of carbon atoms in the alkyl group is 2
4) 100 parts by weight of an unsaturated monomer mixture consisting of 0 to 0.3% by weight of an unsaturated single precipitate selected from θ to 1O (e) 0 to 0.3% by weight of α,β-unsaturated carboxylic acid, 0.1 to 5 parts by weight of emulsifier and 0 to 5 parts of nonionic emulsifier
The film thickness obtained by emulsion polymerization using a polymerization catalyst such as calcium persulfate in the presence of 5 parts by weight is 110~
+80°C.
(a)成分の・・ロゲン基含有不飽和単量体はシェービ
ング屑との密着性を良好とするものであるからできるか
ぎり存在するのが好ましいが、多すぎると乳化重合が困
難となる。Component (a), the unsaturated monomer containing a rogene group, improves adhesion to shaving debris, and is therefore preferably present as much as possible; however, if it is too large, emulsion polymerization becomes difficult.
(b)Fy、分のアクリル酸アルキルエステルは、皮膜
に可撓性を与えるノットモノマーで、アクリル陵エチル
、アクリル酸イングロビル、アクリル酸n・ブチル、ア
クリル酸1−ブチル、アクリル酸n・プロピル、アクリ
ル酸2−エチルヘキシル等が用いられる。(b) Fy, the acrylic acid alkyl ester, is a knot monomer that gives flexibility to the film, including ethyl acrylate, inglovir acrylate, n-butyl acrylate, 1-butyl acrylate, n-propyl acrylate, 2-ethylhexyl acrylate or the like is used.
(C)成分のメタクリル酸メチル、アクリロニトリルま
たはスチレンは皮膜に強靭さを与えるー・−トモツマ−
であ抄、これらの一部をメタクリル酸エチル、メタクリ
ル酸イングロビル、メタクリル酸イソブデルにおきかえ
てもよい。Component (C), methyl methacrylate, acrylonitrile, or styrene, gives toughness to the film.
However, some of these may be replaced with ethyl methacrylate, inglovir methacrylate, or isobutel methacrylate.
(d)成分の一〇H基、−CONHz基、メチロール基
を有する不飽和単量体は(e)成分のカルボキシル基を
有する不飽和酸と同様、シェービング屑との密着性を良
好とするものである。The unsaturated monomer having an 10H group, -CONHz group, and methylol group in component (d) has good adhesion to shaving debris, similar to the unsaturated acid having a carboxyl group in component (e). It is.
(e)成分のα、β−不飽和カルボン酸(その無水物も
含む)としては、アクリル酸、メタクリル酸、イタコン
酸等が利用できる。As the α,β-unsaturated carboxylic acid (including its anhydride) of component (e), acrylic acid, methacrylic acid, itaconic acid, etc. can be used.
アニオン性樹脂水性エマルジョンハ、シェービング屑1
00重量部に対し、樹脂固型分量で8〜50重量部、好
ましくは12〜20重責部の割合で用いる。Anionic resin aqueous emulsion, shaving waste 1
The resin solid content is used in a ratio of 8 to 50 parts by weight, preferably 12 to 20 parts by weight, per 00 parts by weight.
8重を部未満では耐水性の向上に寄与が小さい。If the amount is less than 8 parts, the contribution to the improvement of water resistance is small.
逆に50重量部を越えては皮革調でなく、樹脂ボードの
ような硬いものとなる。On the other hand, if it exceeds 50 parts by weight, it will not have a leather-like appearance but will become hard like a resin board.
エマルジョン中に染料、顔料を配合し、得られる再生皮
革を着色してもよい。又、抄紙時の屑革への樹脂分の塗
着効率の面から、凝集剤を加えても良い。The resulting recycled leather may be colored by adding dyes and pigments to the emulsion. Further, from the viewpoint of the efficiency of coating the resin component on the waste leather during paper making, a flocculant may be added.
実施例
以下、本発明を実施例により更に詳細に説明する。なお
、例中の部および%は特に例記しない限り重量基準であ
る。EXAMPLES Hereinafter, the present invention will be explained in more detail with reference to Examples. Note that parts and percentages in the examples are based on weight unless otherwise specified.
エマルジョンの製造例1
温度調節器、いかり形攪拌器、R流冷却器、供給容器、
幌度計及び窒素導入管を備えた反応容器内に、下記の原
料を装入した。Emulsion production example 1 Temperature controller, anchor stirrer, R flow cooler, supply container,
The following raw materials were charged into a reaction vessel equipped with a hood meter and a nitrogen inlet tube.
水 20
0部エチレンオキシド20モルと反応
させたp−7ニルフエノールの硫
酸中エステルのナトリウム#1(ア
ニオン性乳化剤)の35%水溶液 5部エチレンオ
キシド25モルトfi応
させたp−ノニルフェノール(非
イオン性乳化剤)の20%溶液 20部。water 20
0 parts 35% aqueous solution of sodium #1 ester of p-7 nylphenol in sulfuric acid (anionic emulsifier) reacted with 20 moles of ethylene oxide 5 parts of p-nonylphenol (nonionic emulsifier) reacted with 25 moles of ethylene oxide 20 parts of 20% solution.
次いで、反応容器内を窒素ガスで置換したのち、次に示
す供給物■の10%を加え、混合物を90℃に加熱した
。Next, after purging the inside of the reaction vessel with nitrogen gas, 10% of the following feed (2) was added, and the mixture was heated to 90°C.
供給物I
水 200
部前記アニオン性乳化剤の35%水溶e、 25
部メタクリル酸メチル 195部アクリル
酸n−ブ″fk 189部クロル酢酸ビニ
ル 8部アクリルアミド
8部。Supply I Water 200
Part: 35% aqueous solution of the anionic emulsifier, 25
Parts Methyl methacrylate 195 parts Acrylic acid n-bu''fk 189 parts Vinyl chloroacetate 8 parts Acrylamide
Part 8.
更に185部の水に2.5部の過硫酸カリウムを溶解し
たもの(供給物■)の10%を容器内に装入後、残りの
供給物■全ておよび供給物■の90シを3.5時間かけ
て容器内に供給し、供給終了後、2時間、同温度に保っ
て供給物lを重合させてアニオン性樹脂水性エマルジョ
ンを得た。Furthermore, after charging 10% of a solution of 2.5 parts of potassium persulfate in 185 parts of water (Feed ■) into the container, all of the remaining Feed ■ and 90 parts of Feed ■ were added to 3. The mixture was fed into the container over a period of 5 hours, and after the feeding was completed, the feed L was polymerized while being kept at the same temperature for 2 hours to obtain an anionic resin aqueous emulsion.
例2〜15
ビニル単量体の組成を表1のように変更する他は例1と
同様にしてアニオン性樹脂水性エマルジョンを得た。Examples 2 to 15 Anionic resin aqueous emulsions were obtained in the same manner as in Example 1, except that the composition of the vinyl monomer was changed as shown in Table 1.
実施例1
皮革製造業より発生した廃材であるクロムなめし処理の
シェービング屑(繊維長5■)をスーバ−ミキサーで所
定粒状になるまで粉砕し、これをナイアガラビーターに
4%濃度になる様に仕込んだ。ナイアガラビーターでは
40分間叩解ならびに解繊を行なった。Example 1 Chrome tanning shaving waste (fiber length 5cm), which is waste material generated from the leather manufacturing industry, was ground into a predetermined granule using a super mixer, and then charged into a Niagara beater at a concentration of 4%. is. Beating and defibration were performed using a Niagara beater for 40 minutes.
この叩解液にさらに水を加えて2%濃度にした。Water was further added to this beaten solution to give a concentration of 2%.
製造例1で得た造膜温度が23℃のアニオン性水性エマ
ルジョン(固型分濃度50%、pi(7,5)を前記叩
解液に、シェービング屑の201i!%(樹脂固型分)
となるように攪拌下に混合して抄紙原料スラリーを得た
。The anionic aqueous emulsion obtained in Production Example 1 with a film-forming temperature of 23°C (solid content concentration 50%, pi (7, 5) in the beating liquid, 201i!% (resin solid content) of shaving waste)
A papermaking raw material slurry was obtained by mixing with stirring so that the following results were obtained.
この抄紙原料スラリーの調製後の経過時間における藁屑
の分散状態は次の通りであった。The state of dispersion of straw waste during the elapsed time after the preparation of this papermaking raw material slurry was as follows.
直後 良好、抄紙可能3時間後
良好、
50℃で1日保管 良好、
50℃で2日保管 良好、 1
50℃で7日保管 良好、
この抄紙原料スラリーに8%硫酸バンドを加えてpHを
4に調整後、これを長網多筒式抄紙で抄造し、プレス脱
水し、更に乾燥空気中で乾燥し、肉厚が約2■の再生皮
革を得た。Immediately Good, paper can be made after 3 hours
Good, stored at 50°C for 1 day Good, stored at 50°C for 2 days Good, 1 Stored at 50°C for 7 days Good, 8% sulfuric acid was added to this papermaking raw material slurry to adjust the pH to 4, and then it was made into fourdrinier. Paper was made using a multi-tube paper machine, dehydrated by press, and further dried in dry air to obtain recycled leather with a wall thickness of approximately 2 cm.
この再生皮革の引張強度は48貯/1.5an幅でろ9
3点曲げ強度は1.3Ai’/1.5t1n幅、吸収率
26.3%でらった。The tensile strength of this recycled leather is 48mm/1.5an width9
The three-point bending strength was 1.3Ai'/1.5t1n width, and the absorption rate was 26.3%.
実施例2〜12、比較例1〜5
表2に示す組成の抄紙原料スラリーを用いて開光に示す
物性の再生皮革を得た。Examples 2 to 12, Comparative Examples 1 to 5 Using papermaking raw material slurries having the compositions shown in Table 2, recycled leather having the physical properties shown in the optical spectrum was obtained.
(以下余白)
実施例15、比較例6
実施例1において、シェービング屑として繊維長が2+
a+のものを用い、かつ、エマルジョンとして例1のも
の(実施例16)、または例10のもの(比較例5)を
用いる他は同様にして再生皮革を得た。(Left below) Example 15, Comparative Example 6 In Example 1, the fiber length was 2+ as shaving waste.
Regenerated leather was obtained in the same manner except that a+ product was used and the emulsion of Example 1 (Example 16) or Example 10 (Comparative Example 5) was used.
特許出願人 三菱油化バーディツシエ株式会社代理人
弁理士 長 谷 正 大
同上 山本隆也Patent applicant Mitsubishi Yuka Verdice Co., Ltd. Agent
Patent Attorney Tadashi Hase Daido Takaya Yamamoto
Claims (1)
する屑解繊物と、革のたん白質と反応するクロル基また
はブロム基を有する不飽和単量体0.5〜10重量%と
他の不飽和単量体99.5〜90重量%とを共重合させ
て得た共重合体のアニオン性樹脂水性エマルジョンを含
有するスラリーを抄紙して再生皮革を製造する方法。 2)、アニオン性樹脂水性エマルジョンの共重合体は、 (a)クロル基またはブロム基を有する不飽和単量体0
.5〜10重量% (b)アクリル酸アルキルエステル(アルキル基の炭素
数は2〜8) 40〜55重量、 (c)メタクリル酸メチル、スチレン、アクリロニトリ
ルより選ばれた単量体 30〜55重量% (d)N−フェニルマレイミド、N−メチロールアクリ
ルアミド、アクリルアミド、メタク リルアミド、2−ヒドロキシアルキルアク リレート(アルキル基の炭素数は2〜4) より選ばれた不飽和単量体 0〜10重量、 (e)α,β−不飽和カルボン酸0〜0.3重量%より
なる不飽和単量体混合物100重量部を、アニオン性乳
化剤0.5〜5重量部の存在下に乳化重合して得られた
共重合体である請求項第1項記載の方法。 3)、シェービング屑解繊物100重量部に対し、アニ
オン性樹脂水性エマルジョンが樹脂固型分量で8〜50
重量部の割合で配合されることを特徴とする請求項第1
項記載の方法。[Scope of Claims] 1) A defibrated waste material mainly composed of chrome-tanned leather shavings and an unsaturated monomer having a chloro group or a bromine group that reacts with the protein of the leather. A method for producing recycled leather by making paper from a slurry containing an aqueous emulsion of an anionic resin of a copolymer obtained by copolymerizing 10% by weight and 99.5 to 90% by weight of other unsaturated monomers. 2) The copolymer of the anionic resin aqueous emulsion contains (a) 0 unsaturated monomers having a chloro group or a bromine group.
.. 5 to 10% by weight (b) 40 to 55% by weight of an acrylic acid alkyl ester (alkyl group has 2 to 8 carbon atoms), (c) 30 to 55% by weight of a monomer selected from methyl methacrylate, styrene, and acrylonitrile. (d) 0 to 10 weight unsaturated monomers selected from N-phenylmaleimide, N-methylolacrylamide, acrylamide, methacrylamide, 2-hydroxyalkyl acrylate (alkyl group has 2 to 4 carbon atoms), (e ) Obtained by emulsion polymerization of 100 parts by weight of an unsaturated monomer mixture consisting of 0 to 0.3% by weight of α,β-unsaturated carboxylic acid in the presence of 0.5 to 5 parts by weight of an anionic emulsifier. 2. The method according to claim 1, which is a copolymer. 3) The anionic resin aqueous emulsion has a resin solid content of 8 to 50 parts by weight per 100 parts by weight of defibrated shaving waste.
Claim 1, characterized in that it is blended in the proportion of parts by weight.
The method described in section.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63291916A JPH0751720B2 (en) | 1988-11-18 | 1988-11-18 | Manufacturing method of recycled leather |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63291916A JPH0751720B2 (en) | 1988-11-18 | 1988-11-18 | Manufacturing method of recycled leather |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02138400A true JPH02138400A (en) | 1990-05-28 |
JPH0751720B2 JPH0751720B2 (en) | 1995-06-05 |
Family
ID=17775117
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63291916A Expired - Fee Related JPH0751720B2 (en) | 1988-11-18 | 1988-11-18 | Manufacturing method of recycled leather |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0751720B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4892693A (en) * | 1987-07-24 | 1990-01-09 | Aluminum Company Of America | Method of making filament growth composite |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59560A (en) * | 1982-06-28 | 1984-01-05 | Takayasu Okuno | Sucked gas mixer of internal-combustion engine |
-
1988
- 1988-11-18 JP JP63291916A patent/JPH0751720B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59560A (en) * | 1982-06-28 | 1984-01-05 | Takayasu Okuno | Sucked gas mixer of internal-combustion engine |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4892693A (en) * | 1987-07-24 | 1990-01-09 | Aluminum Company Of America | Method of making filament growth composite |
Also Published As
Publication number | Publication date |
---|---|
JPH0751720B2 (en) | 1995-06-05 |
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